MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability-Reference-Cited by-同舟云学术

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MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability

Published:2023-02 Issue: Volume: Page:
ISSN:1059-1311
Container-title:Seizure
language:en
Short-container-title:Seizure

Author:

Yang Jie-Hua,Liu Zhi-Gang,Liu Chun-Ling,Zhang Ming-Rui,Jia Yan-Lu,Zhai Qiong-Xiang,He Ming-Feng,He Na,Qiao Jing-Da^ORCID

Funder

National Natural Science Foundation of China

Basic and Applied Basic Research Foundation of Guangdong Province

Second Affiliated Hospital of Guangzhou Medical University

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology,General Medicine

Reference26 articles.

1. Mediator is a transducer of Wnt/beta-catenin signaling;Kim;J Biol Chem,2006

2. The SCF-Fbw7 ubiquitin ligase degrades MED13 and MED13L and regulates CDK8 module association with mediator;Davis;Genes Dev,2013

3. Molecular and in vivo functions of the CDK8 and CDK19 kinase modules;Dannappel;Front Cell Dev Biol,2018

4. A precisely positioned MED12 activation helix stimulates CDK8 kinase activity;Klatt;Proc Natl Acad Sci U S A,2020

5. Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling;Rocha;Development.,2010

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1. Epilepsy-associated genes: an update;Seizure: European Journal of Epilepsy;2023-09

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